Canonical Allele Identifier: CA2261182779

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007617T= , CM000679.2:g.44007617T=	GRCh38
NC_000017.10:g.42084985T= , CM000679.1:g.42084985T=	GRCh37
NC_000017.9:g.39440511T=	NCBI36
NG_008106.1:g.7954T=
NG_023338.1:g.1853A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000293404.8:c.1295T= (NAGS) MANE Select	ENSP00000293404.2:p.Met432=
ENST00000293404.7:c.1295T= (NAGS)	ENSP00000293404.2:p.Met432=
ENST00000589767.1:c.1226T= (NAGS)	ENSP00000465408.1:p.Met409=
ENST00000592915.1:n.1183T= (NAGS)
NM_153006.2:c.1295T= (NAGS)	NP_694551.1:p.Met432=
XM_011524438.1:c.1268+123T= (NAGS)	XP_011522740.1:n.1268+123T=
XM_011524439.1:c.797T= (NAGS)	XP_011522741.1:p.Met266=
XM_011525035.1:c.-463+15955A= (PYY)	XP_011523337.1:n.-463+15955A=
XM_011524439.2:c.797T= (NAGS)	XP_011522741.1:p.Met266=
NM_153006.3:c.1295T= (NAGS) MANE Select	NP_694551.1:p.Met432=